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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Hélix-Nielsen, Claus
Technical University of Denmark
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (14/14 displayed)
- 2023Facile Fabrication of Flexible Ceramic Nanofibrous Membranes for Enzyme Immobilization and Transformation of Emerging Pollutantscitations
- 2023Facile Fabrication of Flexible Ceramic Nanofibrous Membranes for Enzyme Immobilization and Transformation of Emerging Pollutantscitations
- 2023Synthesis of magnetic nanoparticles with covalently bonded polyacrylic acid for use as forward osmosis draw agentscitations
- 2022Concentrating hexavalent chromium electroplating wastewater for recovery and reuse by forward osmosis using underground brine as draw solutioncitations
- 2021Employing the synergistic effect between aquaporin nanostructures and graphene oxide for enhanced separation performance of thin-film nanocomposite forward osmosis membranescitations
- 2021Impedance characterization of biocompatible hydrogel suitable for biomimetic lipid membrane applicationscitations
- 2021Impact of sodium hypochlorite on rejection of non-steroidal anti-inflammatory drugs by biomimetic forward osmosis membranescitations
- 2019Synthesis of Poly-Sodium-Acrylate (PSA)-Coated Magnetic Nanoparticles for Use in Forward Osmosis Draw Solutionscitations
- 2016Influence of feed composition and membrane fouling on forward osmosis performance
- 2015A reusable device for electrochemical applications of hydrogel supported black lipid membranescitations
- 2015A feasibility study of ultrafiltration/reverse osmosis (UF/RO)-based wastewater treatment and reuse in the metal finishing industrycitations
- 2012Tailoring Properties of Biocompatible PEG-DMA Hydrogels with UV Lightcitations
- 2011Surface Modifications of Support Partitions for Stabilizing Biomimetic Membrane Arrayscitations
- 2011Electrochemical characterization of hydrogels for biomimetic applicationscitations
Places of action
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article
Electrochemical characterization of hydrogels for biomimetic applications
Abstract
Hydrogels are increasingly being recognized as having potential in bio‐compatible applications. In previous work, we investigated the feasibility of poly(ethylene glycol)‐dimethacrylate (PEG‐1000‐DMA) and poly(ethylene glycol)‐diacrylate (PEG‐400‐DA) polymerized using either a chemical initiator (C) or a photoinitiator (P) to encapsulate and stabilize biomimetic membranes for novel separation technologies or biosensor applications. In this paper, we have investigated the electrochemical properties of the hydrogels used for membrane encapsulation. Specifically, we studied the crosslinked hydrogels by using electrochemical impedance spectroscopy (EIS), and we demonstrated that chemically crosslinked hydrogels had lower values for the effective electrical resistance and higher values for the electrical capacitance compared with hydrogels with photoinitiated crosslinking. Transport numbers were obtained using electromotive force measurements and demonstrated that at low salt concentrations, both PEG‐400‐DA‐C and PEG‐400‐DA‐P hydrogels presented an electropositive character whereas PEG‐1000‐DMA‐P was approximately neutral and PEG‐1000‐DMA‐C showed electronegative character. Sodium transport numbers approached the bulk NaCl electrolyte value at high salt concentrations for all hydrogels, indicating screening of fixed charges in the hydrogels. The average salt diffusional permeability 〈Ps〉 and water permeability 〈Pw〉 were found to correlate with EIS results. Both PEG‐1000‐DMA‐C and PEG‐400‐DA‐C had higher 〈Ps〉 and 〈Pw〉 values than PEG‐1000‐DMA‐P and PEG‐400‐DA‐P hydrogels. In conclusion, our results show that hydrogel electrochemical properties can be controlled by the choice of polymer and type of crosslinking used and that their water and salt permeability properties are congruent with the use of hydrogels for biomimetic membrane encapsulation. Copyright © 2011 John Wiley & Sons, Ltd.